Canonical Allele Identifier: CA483154278
Gene: GJB2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr13:g.20763109C>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.20188970C>G , CM000675.2:g.20188970C>G GRCh38
NC_000013.10:g.20763109C>G , CM000675.1:g.20763109C>G GRCh37
NC_000013.9:g.19661109C>G NCBI36
NG_008358.1:g.9006G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000382844.2:c.612G>C ENSP00000372295.1:p.Leu204=
ENST00000382848.5:c.612G>C MANE Select ENSP00000372299.4:p.Leu204=
ENST00000382844.1:c.612G>C ENSP00000372295.1:p.Leu204=
ENST00000382848.4:c.612G>C ENSP00000372299.4:p.Leu204=
NM_004004.5:c.612G>C NP_003995.2:p.Leu204=
XM_011535049.1:c.612G>C XP_011533351.1:p.Leu204=
XM_011535049.2:c.612G>C XP_011533351.1:p.Leu204=
NM_004004.6:c.612G>C MANE Select NP_003995.2:p.Leu204=